Yafal A G, Palma E L
J Virol. 1979 Jun;30(3):643-9. doi: 10.1128/JVI.30.3.643-649.1979.
The role of procapsids during foot-and-mouth disease virus multiplication was studied on infected BHK-21 cells. Purified virus and procapsids were obtained by treating the infected cytoplasmic extracts with RNase and EDTA. The synthesis of virus, procapsids, and total particles was determined in pulse-chase experiments. A precursor-product relationship between procapsids and virions was obtained. The results show that the rate of synthesis of total particles (virus + procapsids) was linear from the addition of the label and was identical to that corresponding to virions. Therefore, the speed of the morphogenetic process as well as the existence of a precursor pool of structural proteins was established. Furthermore, the rate of virus synthesis from procapsids was identical to the rate of synthesis of procapsids from their structural precursors. A quantitative recovery of label from procapsids into virions was obtained by the use of cycloheximide or tosyl-lysine chloromethyl ketone. Under these conditions, virus synthesis proceeds, indicating that these drugs do not affect the morphogenetic step studied in this paper.
在感染的BHK - 21细胞上研究了原衣壳在口蹄疫病毒增殖过程中的作用。通过用核糖核酸酶和乙二胺四乙酸处理感染的细胞质提取物来获得纯化的病毒和原衣壳。在脉冲追踪实验中测定了病毒、原衣壳和总颗粒的合成情况。得出了原衣壳与病毒粒子之间的前体 - 产物关系。结果表明,从添加标记物开始,总颗粒(病毒 + 原衣壳)的合成速率呈线性,且与病毒粒子的合成速率相同。因此,确定了形态发生过程的速度以及结构蛋白前体池的存在。此外,从原衣壳合成病毒的速率与从其结构前体合成原衣壳的速率相同。通过使用环己酰亚胺或甲苯磺酰赖氨酸氯甲基酮,实现了标记物从原衣壳到病毒粒子的定量回收。在这些条件下,病毒合成继续进行,表明这些药物不影响本文所研究的形态发生步骤。